Diisopropylamine → HCID 10219791, compound
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1.[CH:12]([NH:15]C(C)C)([CH3:14])[CH3:13]>CO>[CH3:13][CH:12]([NH:15][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1)[CH3:14]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
The 3-chloro-1-(3-pyridyloxy)propane (0.80 g, 4.66 mmol) was dissolved in methanol (25 mL) and added to diisopropylamine (25 mL) in a heavy-walled glass pressure-tube apparatus. The tube was sealed and the mixture was stirred and heated at 100° C. (oil bath temperature) for 4 h. After cooling, the mixture was concentrated by rotary evaporation. Saturated NaCl solution (10 mL) was added to the residue, and the solution (pH 6) was extracted with ether (3×25 mL) to remove impurities. The aqueous layer was basified to pH 10 with 100% NaOH solution, and the mixture was extracted with chloroform (4×25 mL). The combined chloroform extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give 0.531 g (58.6%) of a dark-brown oil. The compound exhibits a Ki of 8500 nM. The compound exhibits neurotransmitter release of 16 percent.
Workup
- customThe tube was sealed
- temperatureAfter cooling
- concentrationthe mixture was concentrated by rotary evaporation
- additionSaturated NaCl solution (10 mL) was added to the residue
- extractionthe solution (pH 6) was extracted with ether (3×25 mL)
- customto remove impurities
- extractionthe mixture was extracted with chloroform (4×25 mL)
- dry with materialThe combined chloroform extracts were dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated by rotary evaporation to a residue that
- customwas dried briefly under high vacuum
Sources & evidence
- ORD record
- ord-d89a08f450574b109461dd43a72a86e0
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06441006B2
Reaction notes
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